Abstract
Regio-, stereo-, and chemoselective halofluorination of alkenes is achieved using N-haloamides and tetrabutylammonium dihydrogentrifluoride, and the resulting F-I adducts were successfully converted into fluoroalkenes under dehydroiodination with 1,8-diazabicyclo[5.4.0]undec-7-ene.
Original language | English |
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Pages (from-to) | 1215-1218 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 32 |
Issue number | 9 |
DOIs | |
Publication status | Published - Feb 25 1991 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry